Rapid Determination of Six Anesthetics Residues in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Pass-through Solid Phase Extraction
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Rapid Determination of Six Anesthetics Residues in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Pass-through Solid Phase Extraction
Vol. 38, Issue 9, Pages: 1059-1065(2019)
作者机构:
1. 湛江市食品药品检验所
2. 广东恒兴饲料实业股份有限公司农业农村部华南水产与畜禽饲料重点实验室
3. 广东海洋大学食品科技学院广东省水产品加工与安全重点实验室
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Rapid Determination of Six Anesthetics Residues in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Pass-through Solid Phase Extraction. [J]. 38(9):1059-1065(2019)
DOI:
Rapid Determination of Six Anesthetics Residues in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Pass-through Solid Phase Extraction. [J]. 38(9):1059-1065(2019)DOI:
Rapid Determination of Six Anesthetics Residues in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Pass-through Solid Phase Extraction
A high performance liquid chromatography-tandem mass spectrometric(HPLC-MS/MS) method was developed for the rapid determination of six anesthetics,eg.procaine,lidocaine,bupivacaine,tetracaine,tricaine methanesulfonate(MS-222) and benzocaine in aquatic products.The samples were extracted with water and acetonitrile containing 1.0% formic acid,and then cleaned up with a PRiME HLB pass through solid phase extraction column.The targets were separated on a ZORBAX Eclipse XDB-C18 column(3.0 mm×150 mm,3.5 μm) with acetonitrile-0.1% formic acid as mobile phase by gradient elution.The analytes were determined in electrospray positive ionization(ESI+) mode under multiple reaction monitoring(MRM).Results showed that there were good linear relationships for the targets in their respective concentration ranges with correlation coefficients(r2) of 0.993 8-0.998 7.The limits of detection(LOD) and limits of quantitation(LOQ) were in the ranges of 1.5-6.0 μg/kg and 5.0-20 μg/kg,respectively.Average spiked recoveries for six anesthetics were in the range of 76.8%-110% with relative standard deviations of 4.2%-11%.The proposed method is simple,quick,accurate and sensitive,and is suitable for the determination of six anesthetics in aquatic products.
关键词
麻醉剂通过式固相萃取水产品高效液相色谱-串联质谱(HPLC-MS/MS)
Keywords
anestheticspass-through solid phase extractionaquatic productshigh performance liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)
Research on the Residual Detection of Quinocetone,Cyadox and Their Main Metabolites in Aquatic Products by HPLC-MS/MS
Rapid Detection of Tetrodotoxin in Aquatic Products by Colloidal Gold Immunochromatography Assay
Simultaneous Determination of Ten Tranquilizers and Their Metabolites in Aquatic Products by Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of Ethoxyquinoline and Ethoxyquinoline Dimer in Aquatic Products by High Performance Liquid Chromatography-Tandem Mass Spectrometry
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